Erythromycin Lactobionate Injection, Powder, Lyophilized, For Solution
Product Images NDC 68083-513

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Erythromycin Lactobionate (NDC 68083-513). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gland Pharma Limited, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Erythromycin-carton-label (Erythromycin Carton Label)

Erythromycin-carton-label (Erythromycin Carton Label)
Packaging label for Erythromycin Lactobionate for Injection, USP 500 mg per vial in lyophilized powder form. The label states it contains 10 single-dose vials, benzyl alcohol free formula, for intravenous use only. Manufactured by Gland Pharma Limited, Hyderabad, India, with product NDC 68083-513-10. Instructions include preparation with 10 mL sterile water for injection and storage notes.*
FDA Label Image

Erythromycin-spl-structure (Erythromycin Spl Structure)

Erythromycin-spl-structure (Erythromycin Spl Structure)
Chemical structure diagram of erythromycin lactobionate, showing the molecular arrangement and connectivity with its chemical formula C12H22O12 noted on the image.*
FDA Label Image

Erythromycin-vial-label (Erythromycin Vial Label)

Erythromycin-vial-label (Erythromycin Vial Label)
Label for Erythromycin Lactobionate for Injection, USP, showing 500 mg erythromycin activity per vial in a benzyl alcohol free formula. The product is lyophilized powder for intravenous injection, single-dose vial, manufactured by Gland Pharma Limited, India. Storage instructions and dilution details are provided along with the NDC number 68083-513-01.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.